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Re-engineering clinical trials : best practices for streamlining the development process /

The pharmaceutical industry is currently operating under a business model that is not sustainable for the future. Given the high costs associated with drug development, there is a vital need to reform this process in order to provide safe and effective drugs while still securing a profit. Re-Enginee...

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Bibliographic Details
Corporate Author: ScienceDirect (Online service)
Other Authors: Schüler, Peter, Buckley, Brendan
Format: eBook
Language:English
Published: Amsterdam : Academic Press, 2015.
Subjects:
Drugs > Testing.
Drug development > Safety measures.
Clinical trials.
Drug development > Economic aspects.
Drugs > Design.
Clinical Trials as Topic
Drug Approval
Drug Design
Médicaments > Essais cliniques.
Médicaments > Développement > Sécurité > Mesures.
Études cliniques.
Médicaments > Développement > Aspect économique.
Médicaments > Conception.
MEDICAL > Pharmacology.
Drugs > Design
Clinical trials
Drugs > Testing
Electronic books.
Online Access:Connect to the full text of this electronic book
Description
Summary:The pharmaceutical industry is currently operating under a business model that is not sustainable for the future. Given the high costs associated with drug development, there is a vital need to reform this process in order to provide safe and effective drugs while still securing a profit. Re-Engineering Clinical Trials evaluates the trends and challenges associated with the current drug development process and presents solutions that integrate the use of modern communication technologies, innovations and novel enrichment designs. This book focuses on the need to simplify drug development and ...
Physical Description:1 online resource (383 pages) : illustrations (some color)
Bibliography:Includes bibliographical references and index.
ISBN:9780128007907
0128007907